Detalhe da pesquisa
1.
Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca2+ signaling.
EMBO J
; 39(4): e102363, 2020 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31957048
2.
WWC2 expression in the testis: Implications for spermatogenesis and male fertility.
FASEB J
; 37(5): e22912, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37086090
3.
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Am J Hum Genet
; 107(2): 342-351, 2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32673564
4.
Congenital Limb Defects: A Retrospective Cohort Study and Overview of the Literature.
Ultraschall Med
; 44(5): e241-e247, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36198323
5.
The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA.
J Biol Chem
; 295(38): 13181-13193, 2020 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32703901
6.
Extrinsic immune cell-derived, but not intrinsic oligodendroglial factors contribute to oligodendroglial differentiation block in multiple sclerosis.
Acta Neuropathol
; 140(5): 715-736, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32894330
7.
Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system.
Eur J Nucl Med Mol Imaging
; 47(9): 2131-2141, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31960097
8.
The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.
Hum Mol Genet
; 25(22): 4898-4910, 2016 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28171660
9.
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
N Engl J Med
; 372(22): 2097-107, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25970010
10.
Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.
Med Genet
; 30(1): 12-20, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29527098
11.
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
J Assist Reprod Genet
; 34(5): 683-694, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28401488
12.
Universal cardiac induction of human pluripotent stem cells in two and three-dimensional formats: implications for in vitro maturation.
Stem Cells
; 33(5): 1456-69, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25639979
13.
Action of steroids and plant triterpenoids on CatSper Ca2+ channels in human sperm.
Proc Natl Acad Sci U S A
; 115(3): E344-E346, 2018 01 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29305558
14.
Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.
Urol Int
; 95(4): 386-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25660097
15.
Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report.
Front Med (Lausanne)
; 11: 1340905, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38414622
16.
Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation.
J Clin Invest
; 134(1)2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38165034
17.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Lancet
; 380(9854): 1674-82, 2012 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23020937
18.
Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
Eur Urol
; 83(5): 452-462, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35690514
19.
WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
Am J Hum Genet
; 85(1): 97-105, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19559398
20.
Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome.
Stem Cell Res
; 62: 102826, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35667217